RacF1, a novel member of the Rho protein family in Dictyostelium discoideum, associates transiently with cell contact areas, macropinosomes, and phagosomes

被引:53
作者
Rivero, F
Albrecht, R
Dislich, H
Bracco, E
Graciotti, L
Bozzaro, S
Noegel, AA [1 ]
机构
[1] Univ Cologne, Fak Med, Inst Biochem 1, D-50931 Cologne, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Osped S Luigi Gonzaga, Dipartimento Sci Clin & Biol, I-10043 Turin, Italy
关键词
D O I
10.1091/mbc.10.4.1205
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Using a PCR approach we have isolated racF1, a novel member of the Rho family in Dictyostelium. The racF1 gene encodes a protein of 193 amino acids and is constitutively expressed throughout the Dictyostelium life cycle. Highest identity (94%) was found to a RacF2 isoform, to Dictyostelium Rac1A, Rac1B, and Rac1C (70%), and to Rac proteins of animal species (64 - 69%). To investigate the role of RacF1 in cyto skeleton-dependent processes, we have fused it at its amino-terminus with green fluorescent protein (GFP) and studied the dynamics of subcellular redistribution using a confocal laser scanning microscope and a double-view microscope system. GFP-RacF1 was homogeneously distributed in the cytosol and accumulated at the plasma membrane, especially at regions of transient intercellular contacts. GFP-RacF1 also localized transiently to macropinosomes and phagocytic cups and was gradually released within <1 min after formation of the endocytic vesicle or the phagosome, respectively. On stimulation with cAMP, no enrichment of GFP-RacF1 was observed in leading fronts, from which it was found to be initially excluded. Cell lines were obtained using homologous recombination that expressed a truncated racF1 gene lacking sequences encoding the carboxyl-terminal region responsible for membrane targeting. These cells displayed normal phagocytosis, endocytosis, and exocytosis rates. Our results suggest that RacF1 associates with dynamic structures that are formed during pinocytosis and phagocytosis. Although RacF1 appears not to be essential, it might act in concert and/or share functions with other members of the Rho family in the regulation of a subset of cytoskeletal rearrangements that are required for these processes.
引用
收藏
页码:1205 / 1219
页数:15
相关论文
共 54 条
[1]   ACTIVATION OF THE NADPH OXIDASE INVOLVES THE SMALL GTP-BINDING PROTEIN P21RAC1 [J].
ABO, A ;
PICK, E ;
HALL, A ;
TOTTY, N ;
TEAHAN, CG ;
SEGAL, AW .
NATURE, 1991, 353 (6345) :668-670
[2]   ISOLATION OF DICTYOSTELIUM-DISCOIDEUM CYTOKINESIS MUTANTS BY RESTRICTION ENZYME-MEDIATED INTEGRATION OF THE BLASTICIDIN-S RESISTANCE MARKER [J].
ADACHI, H ;
HASEBE, T ;
YOSHINAGA, K ;
OHTA, T ;
SUTOH, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (03) :1808-1814
[3]   INTRACELLULAR-LOCALIZATION OF THE P21(RHO) PROTEINS [J].
ADAMSON, P ;
PATERSON, HF ;
HALL, A .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :617-627
[4]  
AUBRY L, 1993, J CELL SCI, V105, P861
[5]  
BOKOCH GM, 1994, J BIOL CHEM, V269, P31674
[6]  
BOURNE HR, 1991, NATURE, V349, P117, DOI 10.1038/349117a0
[7]   Inactivation of two Dictyostelium discoideum genes, DdPIK1 and DdPIK2, encoding proteins related to mammalian phosphatidylinositide 3-kinases, results in defects in endocytosis, lysosome to postlysosome transport, and actin cytoskeleton organization [J].
Buczynski, G ;
Grove, B ;
Nomura, A ;
Kleve, M ;
Bush, J ;
Firtel, RA ;
Cardelli, J .
JOURNAL OF CELL BIOLOGY, 1997, 136 (06) :1271-1286
[8]   CLONING AND CHARACTERIZATION OF 7 NOVEL DICTYOSTELIUM-DISCOIDEUM RAC-RELATED GENES BELONGING TO THE RHO-FAMILY OF GTPASES [J].
BUSH, J ;
FRANEK, K ;
CARDELLI, J .
GENE, 1993, 136 (1-2) :61-68
[9]   Identification of two distinct mechanisms of phagocytosis controlled by different Rho GTPases [J].
Caron, E ;
Hall, A .
SCIENCE, 1998, 282 (5394) :1717-1721
[10]   ELECTRON-MICROSCOPIC MAPPING OF MONOCLONAL-ANTIBODIES ON THE TAIL REGION OF DICTYOSTELIUM MYOSIN [J].
CLAVIEZ, M ;
PAGH, K ;
MARUTA, H ;
BALTES, W ;
FISHER, P ;
GERISCH, G .
EMBO JOURNAL, 1982, 1 (08) :1017-1022